Clinical Data Reviewer

hace 5 días


Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

About IQVIA

We are a leading provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our mission is to advance human outcomes by delivering knowledge-driven solutions that enable healthcare companies to improve their performance.

Job Description

As a Clinical Data Reviewer at IQVIA, you will be responsible for reviewing, assessing, and processing safety data and information across service lines. You will work closely with our senior operation team members to ensure compliance with applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines.

Main Responsibilities

  • You will process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
  • Your responsibilities will include performing pharmacovigilance activities, such as collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
  • Compliance with quality, productivity, and delivery standards per project requirements is crucial.
  • You will liaise with different functional team members and healthcare professionals to address project-related issues.
  • You will mentor new team members and support department initiatives as assigned by the manager.

Required Skills and Qualifications

  • A Bachelor's degree in life sciences or a related field is required.
  • Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience, is valuable.
  • Fluency in English, Spanish, and Portuguese is necessary.


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